Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SENSI-TOUCH EPIDURAL ANESTHESIA TRAY

K-Number: K950929 · 1995-05-30

ApplicantSherwood Medical Co.
Decision Date1995-05-30
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

SENSI-TOUCH EPIDURAL ANESTHESIA TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1995-05-30 under 510(k) number K950929. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SENSI-TOUCH EPIDURAL ANESTHESIA TRAY?

SENSI-TOUCH EPIDURAL ANESTHESIA TRAY is a medical device that received FDA 510(k) clearance on 1995-05-30. The listed applicant is Sherwood Medical Co.. The 510(k) number is K950929.

When did SENSI-TOUCH EPIDURAL ANESTHESIA TRAY receive FDA 510(k) clearance?

SENSI-TOUCH EPIDURAL ANESTHESIA TRAY received FDA 510(k) clearance on 1995-05-30, under 510(k) number K950929.

Who is the listed applicant for SENSI-TOUCH EPIDURAL ANESTHESIA TRAY?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SENSI-TOUCH EPIDURAL ANESTHESIA TRAY?

The FDA product code for SENSI-TOUCH EPIDURAL ANESTHESIA TRAY is CAZ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Sherwood Medical Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

View all 191 devices →

Related Devices (Code: CAZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261372Profoject™ LOR SyringeCMT Health PTE., Ltd.K222341Arrow 0.2 Micron Flat Filter, GVSArrow International, LLCK210983BD Epilor SyringeBecton, Dickinson and CompanyK201356Plastic LOR SyringeJiangsu Caina Medical Co.,LtdK202699E-Cath STIM acc. TsuiPAJUNK GmbH MedizintechnologieK190345VPCPAJUNK GmbH Medizintechnologie

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑